Colon Cancer: Gene >> BTNL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340184
Start	180908696:180908696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776813203
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Trp(p.R54W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340184
Start	180908642:180908642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769402531
CDS Mutation	c.106G>A
AA Mutation	p.Ala36Thr(p.A36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340184
Start	180911542:180911542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751803412
CDS Mutation	c.601G>A
AA Mutation	p.Ala201Thr(p.A201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340184
Start	180908778:180908778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242A>G
AA Mutation	p.Tyr81Cys(p.Y81C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340184
Start	180950221:180950221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Cys(p.R394C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340184
Start	180950193:180950193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340184
Start	180911370:180911370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148878394
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340184
Start	180908641:180908641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371053690
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340184
Start	180911425:180911425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340184
Start	180947580:180947580(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.747delT
AA Mutation	p.Phe249LeufsTer6(p.F249Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BTNL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340184
Start	180911402:180911402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461G>C
AA Mutation	p.Cys154Ser(p.C154S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript